| Identification | Back Directory | [Name]
2-PIPERIDIN-4-YL-1H-BENZOIMIDAZOLE | [CAS]
38385-95-4 | [Synonyms]
AKOS BBS-00005832
TIMTEC-BB SBB002504
CHEMBRDG-BB 4003376
Bilastine impurity H
OTAVA-BB BB7020410139
Bilasten intermediate 1
2-(4-Piperidinyl)benzimidazole
2-(4-Piperidyl)-1H-benzoimidazole
2-PIPERIDIN-4-YL-1H-BENZIMIDAZOLE
2-PIPERIDIN-4-YL-1H-BENZOIMIDAZOLE
2-(4-piperidinyl)-1H-benzimidazole
1H-BenziMidazole,2-(4-piperidinyl)-
2-(4-PIPERIDYL)-1H-1,3-BENZIMIDAZOLE
2-(PIPERIDIN-4-YL)-1H-BENZO[D]IMIDAZOLE
2-piperidin-4-yl-1H-benzimidazole(SALTDATA: 2HCl 0.5H2O) | [EINECS(EC#)]
609-547-5 | [Molecular Formula]
C12H15N3 | [MDL Number]
MFCD01475843 | [MOL File]
38385-95-4.mol | [Molecular Weight]
201.27 |
| Chemical Properties | Back Directory | [Melting point ]
230 °C (decomp)(Solv: water (7732-18-5)) | [Boiling point ]
441.3±38.0 °C(Predicted) | [density ]
1.167±0.06 g/cm3(Predicted) | [vapor pressure ]
0Pa at 25℃ | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
soluble in Methanol | [form ]
Solid | [pka]
11.83±0.10(Predicted) | [color ]
White to Light yellow to Light orange | [λmax]
279nm(MeOH)(lit.) |
| Hazard Information | Back Directory | [Uses]
2-Piperidin-4-yl-1H-benzimidazole is used as a reagent in the synthesis of 3-amino-1-(5-indanyloxy)-2-propanol derivatives as potent sodium channel blockers for the treatment of ischemic stroke. Also used as a reagent in the synthesis of 2,3,5-trisubstituted pyridine derivatives as potent Akt1/Akt2 dual inhibitors. |
|
|